3-Nitrophenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a nitrophenyl moiety. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents such as dichloromethane and ethanol, while being less soluble in water. The presence of the nitro group (-NO2) on the phenyl ring enhances its reactivity, making it useful in various organic synthesis applications, particularly in Suzuki-Miyaura cross-coupling reactions. The pinacol ester functionality provides stability to the boronic acid group, allowing for easier handling and storage. Additionally, this compound can serve as a building block in the synthesis of more complex organic molecules, including pharmaceuticals and agrochemicals. Its reactivity and functional versatility make it a valuable intermediate in synthetic organic chemistry. Safety precautions should be observed when handling this compound, as with many organoboron compounds, due to potential toxicity and environmental concerns.

3-Nitrophenylboronic acid pinacol ester

68716-48-3: 1,3,2-Dioxaborolane, 4,4,5,5-Tetramethyl-2-(3-Nitrophenyl)-, 4,4,5,5-Tetramethyl-2-(3-nitrophenyl)-1,3,2-dioxaborolane, 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Nitrobenzene

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CAS 68716-48-3: 3-Nitrophenylboronic acid pinacol ester

3-Nitrophenylboronic acid pinacolester

Ref: 3D-FN149684

4,4,5,5-Tetramethyl-2-(3-nitrophenyl)-1,3,2-dioxaborolane

Ref: IN-DA005OLB

4,4,5,5-Tetramethyl-2-(3-nitrophenyl)-1,3,2-dioxaborolane

Ref: 54-OR310399

3-Nitrophenylboronic acid pinacol ester

Ref: 10-F211971